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MaxCare 8910-118 205*118*17cm

by Vevia Finland Oy EUDAMED

Active European Union

Ref MaxCare

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6429810258HY210369 Basic UDI-DIDate30 Nov 2021RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
MaxCare
Model / Reference
MaxCare
Primary DI / UDI-DI
06429810258137
Basic UDI-DI
6429810258HY210369
Direct Marketing DI
06429810258137
EMDN Code
V080702 Non active anti-decubitus medical mattresses
Device Class
Class I
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000006502

Other devices from Vevia Finland Oy

See all devices from Vevia Finland Oy →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No